Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372343Generated: October 26, 2026

Boron trifluoride etherate → 2-(4-Chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone

https://huagongshe.com/reaction/372343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant2-Hydroxy-N-methylacetamideHCID 223579—
Reactant2-(4-Chloro-2-methylphenoxy)acetaldehydeHCID 12391459—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinoneHCID 1239149311%

Reaction Steps

4.6g (0.0325 mole) of boron trifluoride etherate was added to a solution containing 4.6g (0.025 mole) of (4-chloro-2-methylphenoxy)acetaldehyde and 2.5g (0.028 mole) of N-methylglycolamide in 40 ml of tetrahydrofuran. After 24 hours at ambient temperature, the reaction mixture was concentrated under reduced pressure, extracted with ether, washed with water and dried. Purification by silica chromatography gave 0.7g of 2-(4-chloro-2-methylphenoxymethyl)-3-methyl-4-oxazolidinone as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04090861
Source datasetuspto-grants-1978_05
ORD IDord-ed8fab216ce34f0aa59814b2c1f56593
Source noteuspto-grants-1978_05